| Year |
Citation |
Score |
| 2023 |
Tammisetti R, Chaudhari PD, Hong BC, Chien SY. From citronellal to iridoids: asymmetric synthesis of iridoids and their analogues organocatalytic intramolecular Michael reactions. Organic & Biomolecular Chemistry. PMID 37132457 DOI: 10.1039/d3ob00439b |
0.469 |
|
| 2022 |
Tammisetti R, Hong BC, Chien SY, Lee GH. Stereoselective Cyclization Cascade of Dihydroquinoxalinones by Visible-Light Photocatalysis: Access to the Polycyclic Quinoxalin-2(1)-ones. Organic Letters. 24: 5155-5160. PMID 35802069 DOI: 10.1021/acs.orglett.2c01991 |
0.348 |
|
| 2022 |
Lo CL, Akula PS, Hong BC, Lee GH, Chien SY. Total Synthesis of Ulodione A via a Double-Alkylation and DABCO Promoted Ring-Expansion Rearrangement Sequence. Organic Letters. PMID 35499378 DOI: 10.1021/acs.orglett.2c01038 |
0.422 |
|
| 2022 |
Hsu YY, Luo SQ, Hong BC, Chien SY. A mild one-pot transformation of nitroalkanes to ketones or aldehydes a visible-light photocatalysis-hydrolysis sequence. Organic & Biomolecular Chemistry. PMID 35388394 DOI: 10.1039/d2ob00267a |
0.326 |
|
| 2021 |
Akula PS, Wang YJ, Hong BC, Lee GH, Chien SY. Control of the Organocatalytic Enantioselective α-Alkylation of Vinylogous Carbonyl Enolates for the Synthesis of Tetrahydropyran Derivatives and Beyond. Organic Letters. PMID 34048266 DOI: 10.1021/acs.orglett.1c01426 |
0.36 |
|
| 2020 |
Hong BC. Enantioselective synthesis enabled by visible light photocatalysis. Organic & Biomolecular Chemistry. PMID 32458948 DOI: 10.1039/D0Ob00759E |
0.448 |
|
| 2019 |
Jao TJ, Akula PS, Hong BC, Lee GH. Catalytic 1,2-Rearrangements: Organocatalyzed Michael/Semi-Pinacol-like Rearrangement Cascade of 1,3-Diones and Nitroolefins. Organic Letters. PMID 31829018 DOI: 10.1021/Acs.Orglett.9B03912 |
0.499 |
|
| 2019 |
Li YH, Akula PS, Hong BC, Peng CH, Lee GH. Direct Transformation of Nitroalkanes to Nitriles Enabled by Visible-Light Photoredox Catalysis and a Domino Reaction Process. Organic Letters. PMID 31513414 DOI: 10.1021/Acs.Orglett.9B02682 |
0.44 |
|
| 2019 |
Chaudhari PD, Hong BC, Wen CL, Lee GH. Asymmetric Synthesis of Spirocyclopentane Oxindoles Containing Four Consecutive Stereocenters and Quaternary α-Nitro Esters via Organocatalytic Enantioselective Michael-Michael Cascade Reactions. Acs Omega. 4: 655-667. PMID 31459355 DOI: 10.1021/acsomega.8b03049 |
0.438 |
|
| 2019 |
Kao HK, Lin XJ, Hong BC, Yang VW, Lee GH. Enantioselective Synthesis of Yohimbine Analogs by an Organocatalytic and Pot-economic Strategy. The Journal of Organic Chemistry. PMID 31291725 DOI: 10.1021/Acs.Joc.9B01193 |
0.527 |
|
| 2018 |
Akula PS, Hong BC, Lee GH. Visible-light-induced C(sp)-H activation for a C-C bond forming reaction of 3,4-dihydroquinoxalin-2(1)-one with nucleophiles using oxygen with a photoredox catalyst or under catalyst-free conditions. Rsc Advances. 8: 19580-19584. PMID 35540997 DOI: 10.1039/c8ra03259a |
0.346 |
|
| 2018 |
Akula PS, Hong BC, Lee GH. Catalyst- and Substituent-Controlled Switching of Chemoselectivity for the Enantioselective Synthesis of Fully Substituted Cyclobutane Derivatives via 2 + 2 Annulation of Vinylogous Ketone Enolates and Nitroalkene. Organic Letters. PMID 30525690 DOI: 10.1021/Acs.Orglett.8B03335 |
0.501 |
|
| 2018 |
Akula PS, Hong B, Lee G. Visible-light-induced C(sp3)–H activation for a C–C bond forming reaction of 3,4-dihydroquinoxalin-2(1H)-one with nucleophiles using oxygen with a photoredox catalyst or under catalyst-free conditions Rsc Advances. 8: 19580-19584. DOI: 10.1039/C8Ra03259A |
0.436 |
|
| 2017 |
Chaudhari PD, Hong BC, Lee GH. Organocatalytic Enantioselective Michael-Michael-Michael-Aldol Condensation Reactions: Control of Six Stereocenters in a Quadruple-Cascade Asymmetric Synthesis of Polysubstituted Spirocyclic Oxindoles. Organic Letters. PMID 29090937 DOI: 10.1021/Acs.Orglett.7B02962 |
0.549 |
|
| 2017 |
Hsieh YY, Raja A, Hong BC, Kotame P, Chang WC, Lee GH. Organocatalytic Enantioselective Michael-Acetalization-Henry Reaction Cascade of 2-Hydroxynitrostyrene and 5-Oxohexanal for the Entry to the Hexahydro-6H-benzo[c]chromenones with Four Consecutive Stereogenic Centers and an Approach to Aflatoxin Analogues. The Journal of Organic Chemistry. PMID 29065686 DOI: 10.1021/Acs.Joc.7B02178 |
0.529 |
|
| 2017 |
Huang WL, Raja A, Hong BC, Lee GH. Organocatalytic Enantioselective Michael-Acetalization-Reduction-Nef Reaction for a One-Pot Entry to the Functionalized Aflatoxin System. Total Synthesis of (-)- Dihydroaflatoxin D2 and (-)- and (+)-Microminutinin. Organic Letters. PMID 28608693 DOI: 10.1021/Acs.Orglett.7B01473 |
0.53 |
|
| 2017 |
Sheth VM, Hong BC, Lee GH. Enantioselective total synthesis of (+)-arborescidine C and related tetracyclic indole alkaloids using organocatalysis. Organic & Biomolecular Chemistry. PMID 28382347 DOI: 10.1039/C7Ob00473G |
0.517 |
|
| 2016 |
Raja A, Hong BC, Liao JH, Lee GH. Organocatalytic Enantioselective Michael-Michael-Henry Reaction Cascade. An Entry to Highly Functionalized Hajos-Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons. Organic Letters. 18: 1760-3. PMID 27080342 DOI: 10.1021/Acs.Orglett.6B00459 |
0.463 |
|
| 2016 |
Peng C, Hong B, Raja A, Chang C, Lee G. Constructing densely functionalized Hajos–Parrish-type ketones with six contiguous stereogenic centers and two quaternary carbons in a formal [2 + 2 + 2] cycloaddition cascade Rsc Advances. 6: 95314-95319. DOI: 10.1039/C6Ra22430J |
0.389 |
|
| 2016 |
Lin CH, Hong BC, Lee GH. Asymmetric synthesis of functionalized pyrrolizidines by an organocatalytic and pot-economy strategy Rsc Advances. 6: 8243-8247. DOI: 10.1039/C5Ra25103F |
0.514 |
|
| 2016 |
Hong B, Raja A, Sheth VM. ChemInform Abstract: Asymmetric Synthesis of Natural Products and Medicinal Drugs Through One-Pot-Reaction Strategies Cheminform. 47. DOI: 10.1002/CHIN.201601230 |
0.349 |
|
| 2016 |
Chen C, Hong B, Li W, Chang T, Lee G. Synthesis Of Biologically Active Bis(Indolyl)Methane Derivatives by Bisindole Alkylation of Tetrahydroisoquinolines with Visible‐Light Induced Ring‐Opening Fragmentation. Asian Journal of Organic Chemistry. 6: 426-431. DOI: 10.1002/Ajoc.201600415 |
0.462 |
|
| 2015 |
Yang VW, Hong BC, Kao HK, Tu TH, Shen JY, Chen CL, Lee GH, Chou PT. One-Pot Dichotomous Construction of Inside-Azayohimban and Pro-Azayohimban Systems via an Enantioselective Organocatalytic Cascade; Their Use as a Model to Probe the (Aza-)Indole Local Solvent Environment. Organic Letters. PMID 26584631 DOI: 10.1021/Acs.Orglett.5B02949 |
0.462 |
|
| 2015 |
Lin CW, Hong BC, Chang WC, Lee GH. Correction to "A New Approach to Nitrones through Cascade Reaction of Nitro Compounds Enabled by Visible Light Photoredox Catalysis". Organic Letters. PMID 26075499 DOI: 10.1021/Acs.Orglett.5B01663 |
0.389 |
|
| 2015 |
Lin CW, Hong BC, Chang WC, Lee GH. A New Approach to Nitrones through Cascade Reaction of Nitro Compounds Enabled by Visible Light Photoredox Catalysis. Organic Letters. 17: 2314-7. PMID 25895096 DOI: 10.1021/Acs.Orglett.5B00684 |
0.461 |
|
| 2015 |
Hong B, Raja A, Sheth VM. Asymmetric Synthesis of Natural Products and Medicinal Drugs through One-Pot-Reaction Strategies Synthesis. 47: 3257-3285. DOI: 10.1055/S-0035-1560344 |
0.511 |
|
| 2014 |
Raja A, Hong BC, Lee GH. Organocatalytic enantioselective Michael-Michael-Michael-aldol condensation reactions: control of five stereocenters in a quadruple-cascade asymmetric synthesis of highly functionalized hexahydrophenanthrenes. Organic Letters. 16: 5756-9. PMID 25337635 DOI: 10.1021/Ol502821E |
0.54 |
|
| 2014 |
Hsu YH, Chen YA, Tseng HW, Zhang Z, Shen JY, Chuang WT, Lin TC, Lee CS, Hung WY, Hong BC, Liu SH, Chou PT. Locked ortho- and para-core chromophores of green fluorescent protein; dramatic emission enhancement via structural constraint. Journal of the American Chemical Society. 136: 11805-12. PMID 25075971 DOI: 10.1021/Ja5062856 |
0.303 |
|
| 2014 |
Jhuo DH, Hong BC, Chang CW, Lee GH. One-pot organocatalytic enantioselective Michael-Michael-aldol-Henry reaction cascade. A facile entry to the steroid system with six contiguous stereogenic centers. Organic Letters. 16: 2724-7. PMID 24796861 DOI: 10.1021/Ol501011T |
0.529 |
|
| 2014 |
Dange NS, Hong BC, Lee GH. One-pot biomimetic total synthesis of yuehchukene via the organocatalytic alkylation-cyclization process of a sterically encumbered α-alkyl enal Rsc Advances. 4: 59706-59715. DOI: 10.1039/C4Ra10222C |
0.49 |
|
| 2014 |
Raja A, Hong BC, Lee GH. Organocatalytic enantioselective michael-michael-michael-aldol condensation reactions: Control of five stereocenters in a quadruple-cascade asymmetric synthesis of highly functionalized hexahydrophenanthrenes Organic Letters. 16: 5756-5759. DOI: 10.1021/ol502821e |
0.457 |
|
| 2013 |
Hong BC, Lin CW, Liao WK, Lee GH. Sequential asymmetric catalysis in Michael-Michael-Michael-aldol reactions: merging organocatalysis with photoredox catalysis in a one-pot enantioselective synthesis of highly functionalized decalines bearing a quaternary carbon stereocenter. Organic Letters. 15: 6258-61. PMID 24266326 DOI: 10.1021/Ol403113C |
0.487 |
|
| 2013 |
Dange NS, Hong BC, Lee CC, Lee GH. One-pot asymmetric synthesis of seven-membered carbocycles cyclohepta[b]indoles via a sequential organocatalytic Michael/double Friedel-Crafts alkylation reaction Organic Letters. 15: 3914-3917. PMID 23848568 DOI: 10.1021/Ol4016749 |
0.54 |
|
| 2013 |
Hong BC, Liao WK, Dange NS, Liao JH. One-pot organocatalytic enantioselective domino double-Michael reaction and Pictet-Spengler-lactamization reaction. A facile entry to the "inside yohimbane" system with five contiguous stereogenic centers. Organic Letters. 15: 468-71. PMID 23311855 DOI: 10.1021/Ol3032329 |
0.532 |
|
| 2013 |
Hong BC, Lan DJ, Dange NS, Lee GH, Liao JH. Organocatalytic enantioselective Michael-Henry acetalization of glutaraldehyde and 3-aryl-2-nitroprop-2-enols: A facile entry to 3-oxabicyclo[3.3.1]nonan-2-ones with four consecutive stereogenic centers European Journal of Organic Chemistry. 2472-2478. DOI: 10.1002/Ejoc.201201496 |
0.508 |
|
| 2012 |
Hong BC, Dange NS, Yen PJ, Lee GH, Liao JH. Organocatalytic asymmetric anti-selective Michael reactions of aldehydes and the sequential reduction/lactonization/Pauson-Khand reaction for the enantioselective synthesis of highly functionalized hydropentalenes. Organic Letters. 14: 5346-9. PMID 23035862 DOI: 10.1021/Ol302527Z |
0.537 |
|
| 2012 |
Hong BC, Chen PY, Kotame P, Lu PY, Lee GH, Liao JH. Organocatalyzed Michael-Henry reactions: enantioselective synthesis of cyclopentanecarbaldehydes via the dienamine organocatalysis of a succinaldehyde surrogate. Chemical Communications (Cambridge, England). 48: 7790-2. PMID 22714728 DOI: 10.1039/C2Cc33309K |
0.566 |
|
| 2012 |
Hong BC, Dange NS, Ding CF, Liao JH. Organocatalytic Michael-Knoevenagel-hetero-Diels-Alder reactions: an efficient asymmetric one-pot strategy to isochromene pyrimidinedione derivatives. Organic Letters. 14: 448-51. PMID 22195677 DOI: 10.1021/Ol202877M |
0.534 |
|
| 2012 |
Hong BC, Hsu CS, Lee GH. Enantioselective total synthesis of (+)-galbulin via organocatalytic domino Michael-Michael-aldol condensation. Chemical Communications (Cambridge, England). 48: 2385-7. PMID 22179766 DOI: 10.1039/C2Cc16682H |
0.51 |
|
| 2012 |
Hong BC, Hsu CS, Lee GH. Enantioselective total synthesis of (+)-galbulin via organocatalytic domino Michael-Michael-aldol condensation Chemical Communications. 48: 2385-2387. DOI: 10.1039/c2cc16682h |
0.423 |
|
| 2012 |
Hong BC, Dange NS, Ding CF, Liao JH. Organocatalytic Michael-Knoevenagel-hetero-Diels-Alder reactions: An efficient asymmetric one-pot strategy to isochromene pyrimidinedione derivatives Organic Letters. 14: 448-451. DOI: 10.1021/ol202877m |
0.445 |
|
| 2012 |
Hon YS, Luo CZ, Hong BC, Liao JH. Development of the Ireland-Claisen rearrangement of allyl-2-alkoxyacetate bearing an allylic amine and the transformation to 3-hydroxy-4- hydroxymethylpyrrolidine Journal of the Chinese Chemical Society. 59: 273-282. DOI: 10.1002/Jccs.201100630 |
0.422 |
|
| 2012 |
Hon YS, Hong YC, Hong BC, Liao JH. The first synthesis of natural occurring juncaceae coumarin, 9-hydroxy-8-methyl-3H-benzo[f]chromen-3-one, featuring a one-pot rearrangement and aromatization cascade Journal of the Chinese Chemical Society. 59: 407-420. DOI: 10.1002/Jccs.201100481 |
0.412 |
|
| 2011 |
Hong BC, Kotame P, Lee GH. Asymmetric synthesis of 3,4-dihydrocoumarin motif with an all-carbon quaternary stereocenter via a Michael-acetalization sequence with bifunctional amine-thiourea organocatalysts. Organic Letters. 13: 5758-61. PMID 21985707 DOI: 10.1021/Ol202331J |
0.464 |
|
| 2011 |
Hong BC, Dange NS, Hsu CS, Liao JH, Lee GH. Dynamic kinetic asymmetric synthesis of five contiguous stereogenic centers by sequential organocatalytic stetter and Michael-aldol reaction: enantioselective synthesis of fully substituted cyclopentanols bearing a quaternary stereocenter. Organic Letters. 13: 1338-41. PMID 21348455 DOI: 10.1021/Ol200006E |
0.545 |
|
| 2011 |
Hong BC, Nimje RY, Lin CW, Liao JH. Enantioselective organocatalytic Michael-Wittig-Michael-Michael reaction: dichotomous construction of pentasubstituted cyclopentanecarbaldehydes and pentasubstituted cyclohexanecarbaldehydes. Organic Letters. 13: 1278-81. PMID 21348453 DOI: 10.1021/Ol1030487 |
0.504 |
|
| 2011 |
Hong BC, Kotame P, Liao JH. Enantioselective organocatalytic domino Michael-acetalization-Henry reactions of 2-hydroxynitrostyrene and aldehyde for the synthesis of tetrahydro-6H-benzo[c]chromenones. Organic & Biomolecular Chemistry. 9: 382-6. PMID 21088771 DOI: 10.1039/C0Ob00834F |
0.514 |
|
| 2011 |
Hong BC, Sadani AA, Nimje RY, Dange NS, Lee GH. Organocatalytic domino double Michael reaction of ethyl (E)-7-oxohept-2-enoate and ,-unsaturated aldehydes: Efficient asymmetric synthesis of cyclohexanes with four contiguous stereocenters Synthesis. 1887-1895. DOI: 10.1055/S-0030-1260469 |
0.487 |
|
| 2011 |
Hong BC, Kotame P, Liao JH. Enantioselective organocatalytic domino Michael-acetalization-Henry reactions of 2-hydroxynitrostyrene and aldehyde for the synthesis of tetrahydro-6H-benzo[c]chromenones Organic and Biomolecular Chemistry. 9: 382-386. DOI: 10.1039/c0ob00834f |
0.439 |
|
| 2011 |
Hong BC, Kotame P, Lee GH. Asymmetric synthesis of 3,4-dihydrocoumarin motif with an all-carbon quaternary stereocenter via a michael-acetalization sequence with bifunctional amine-thiourea organocatalysts Organic Letters. 13: 5758-5761. DOI: 10.1021/ol202331j |
0.375 |
|
| 2011 |
Hong BC, Dange NS, Hsu CS, Liao JH, Lee GH. Dynamic kinetic asymmetric synthesis of five contiguous stereogenic centers by sequential organocatalytic stetter and Michael-Aldol reaction: Enantioselective synthesis of fully substituted cyclopentanols bearing a quaternary stereocenter Organic Letters. 13: 1338-1341. DOI: 10.1021/ol200006e |
0.462 |
|
| 2011 |
Hong BC, Nimje RY, Lin CW, Liao JH. Enantioselective organocatalytic Michael-Wittig-Michael-Michael reaction: Dichotomous construction of pentasubstituted cyclopentanecarbaldehydes and pentasubstituted cyclohexanecarbaldehydes Organic Letters. 13: 1278-1281. DOI: 10.1021/ol1030487 |
0.392 |
|
| 2010 |
Hong BC, Dange NS, Hsu CS, Liao JH. Sequential organocatalytic Stetter and Michael-Aldol condensation reaction: asymmetric synthesis of fully substituted cyclopentenes via a [1 + 2 + 2] annulation strategy. Organic Letters. 12: 4812-5. PMID 20936853 DOI: 10.1021/Ol101969T |
0.546 |
|
| 2010 |
Hong BC, Kotame P, Tsal CW, Liao JH. Enantioselective total synthesis of (+)-conicol via cascade three-component organocatalysis Organic Letters. 12: 776-779. PMID 20078081 DOI: 10.1021/Ol902840X |
0.519 |
|
| 2010 |
Hong BC, Dange NS, Hsu CS, Liao JH. Sequential organocatalytic stetter and michael-aldol condensation reaction: Asymmetric synthesis of fully substituted cyclopentenes via a [1 + 2 + 2] annulation strategy Organic Letters. 12: 4812-4815. DOI: 10.1021/ol101969t |
0.455 |
|
| 2009 |
Hong BC, Jan RH, Tsai CW, Nimje RY, Liao JH, Lee GH. Organocatalytic enantioselective cascade michael-michael-wittig reactions of phosphorus ylides: One-pot synthesis of the all-cis trisubstituted cyclohexenecarboxylates via the [1+2 + 3] annulation Organic Letters. 11: 5246-5249. PMID 19852490 DOI: 10.1021/Ol9021832 |
0.522 |
|
| 2009 |
Hong BC, Nimje RY, Liao JH. Enantioselective synthesis of highly functionalized octahydro-6-oxo-1- phenylnaphthalene-2-carbaldehydes via organocatalytic domino reactions Organic and Biomolecular Chemistry. 7: 3095-3101. DOI: 10.1039/B906205J |
0.478 |
|
| 2009 |
Kotame P, Hong BC, Liao JH. Enantioselective synthesis of the tetrahydro-6H-benzo[c]chromenes via Domino Michael-Aldol condensation: control of five stereocenters in a quadruple-cascade organocatalytic multi-component reaction Tetrahedron Letters. 50: 704-707. DOI: 10.1016/J.Tetlet.2008.11.106 |
0.485 |
|
| 2009 |
Kotame P, Hong B, Liao J. ChemInform Abstract: Enantioselective Synthesis of the Tetrahydro-6H-benzo[c]chromenes via Domino Michael-Aldol Condensation: Control of Five Stereocenters in a Quadruple-Cascade Organocatalytic Multi-Component Reaction. Cheminform. 40. DOI: 10.1002/CHIN.200921136 |
0.405 |
|
| 2008 |
Hong BC, Nimje RY, Sadani AA, Liao JH. Organocatalytic enantioselective domino Michael-aldol condensation of 5-oxoalkanal and alpha,beta-unsaturated aldehydes. Efficient assembly of densely functionalized cyclohexenes. Organic Letters. 10: 2345-8. PMID 18484729 DOI: 10.1021/Ol8005369 |
0.486 |
|
| 2008 |
Hong BC, Nimje RY, Sadani AA, Liao JH. Organocatalytic enantioselective domino michael-aldol condensation of 5-oxoalkanal and α,β-unsaturated aldehydes. Efficient assembly of densely functionalized cyclohexenes Organic Letters. 10: 2345-2348. DOI: 10.1021/ol8005369 |
0.398 |
|
| 2008 |
Hong BC, Liu KL, Tsai CW, Liao JH. Proline-mediated dimerization of cinnamaldehydes via 1,3-dipolar cycloaddition reaction with azomethine ylides. A rapid access to highly functionalized hexahydro-1H-pyrrolizine Tetrahedron Letters. 49: 5480-5483. DOI: 10.1016/J.Tetlet.2008.07.039 |
0.469 |
|
| 2008 |
Hong BC, Nimje RY, Wu MF, Sadani AA. Organocatalytic double Michael reaction of 7-oxohept-2-enoates and nitrostyrene - Formal synthesis of (-)-α- and (-)-β-lycorane European Journal of Organic Chemistry. 1449-1457. DOI: 10.1002/Ejoc.200701122 |
0.455 |
|
| 2007 |
Hong BC, Wu MF, Tseng HC, Huang GF, Su CF, Liao JH. Organocatalytic asymmetric robinson annulation of alpha,beta-unsaturated aldehydes: applications to the total synthesis of (+)-palitantin. The Journal of Organic Chemistry. 72: 8459-71. PMID 17919000 DOI: 10.1021/Jo701477V |
0.473 |
|
| 2007 |
Hong BC, Nimje RY, Yang CY. The organocatalytic direct self-trimerization of acrolein: application to the total synthesis of montiporyne F Tetrahedron Letters. 48: 1121-1125. DOI: 10.1016/J.Tetlet.2006.12.055 |
0.386 |
|
| 2007 |
Hong BC, Tseng HC, Chen SH. Synthesis of aromatic aldehydes by organocatalytic [4+2] and [3+3] cycloaddition of α,β-unsaturated aldehydes Tetrahedron. 63: 2840-2850. DOI: 10.1016/J.Tet.2007.01.039 |
0.404 |
|
| 2006 |
Hong BC, Wu MF, Tseng HC, Liao JH. Enantioselective organocatalytic formal [3 + 3]-cycloaddition of alpha,beta-unsaturated aldehydes and application to the asymmetric synthesis of (-)-isopulegol hydrate and (-)-cubebaol. Organic Letters. 8: 2217-20. PMID 16706490 DOI: 10.1021/Ol060486+ |
0.425 |
|
| 2006 |
Hong BC, Hallur MS, Liao JH. Hetero Diels-Alder cycloaddition of indene for the formal synthesis of onychnine Synthetic Communications. 36: 1521-1528. DOI: 10.1080/00397910600588520 |
0.392 |
|
| 2006 |
Hong BC, Kim S, Kim TS, Corey EJ. Synthesis and properties of several isomers of the cardioactive steroid ouabain Tetrahedron Letters. 47: 2711-2715. DOI: 10.1016/J.Tetlet.2006.02.089 |
0.525 |
|
| 2006 |
Tseng HC, Gupta AK, Hong BC, Liao JH. Regioselective electrophilic substitutions of fulvenes with ethyl glyoxylate and subsequent Diels-Alder reactions Tetrahedron. 62: 1425-1432. DOI: 10.1016/J.Tet.2005.11.029 |
0.516 |
|
| 2006 |
Hong B, Jiang Y, Chang Y, Lee S. Synthesis and Cytotoxicity Studies of Cyclohepta[b]indoles, Benzo[6,7]Cyclohepta[1,2-b]Indoles, Indeno[1,2-b]Indoles, and Benzo[a]Carbazoles Journal of the Chinese Chemical Society. 53: 647-662. DOI: 10.1002/Jccs.200600086 |
0.331 |
|
| 2005 |
Hong BC, Chen ZY, Nagarajan A, Kottani R, Chavan V, Chen WH, Jiang YF, Zhang SC, Liao JH, Sarshar S. Efficient and stereodivergent synthesis of deoxyimino sugars. Carbohydrate Research. 340: 2457-68. PMID 16169539 DOI: 10.1016/J.Carres.2005.08.014 |
0.498 |
|
| 2005 |
Hong BC, Chen FL, Chen SH, Liao JH, Lee GH. Intramolecular Diels-Alder cycloadditions of fulvenes. Application to the kigelinol, neoamphilectane, and kempane skeletons Organic Letters. 7: 557-560. PMID 15704893 DOI: 10.1021/Ol047730M |
0.383 |
|
| 2005 |
Chen SH, Hong BC, Su CF, Sarshar S. An unexpected inversion of enantioselectivity in the proline catalyzed intramolecular Baylis-Hillman reaction Tetrahedron Letters. 46: 8899-8903. DOI: 10.1016/J.Tetlet.2005.10.072 |
0.497 |
|
| 2005 |
Hong BC, Chen ZY, Nagarajan A, Rudresha K, Chavan V, Chen WH, Jiang YF, Zhang SC, Lee GH, Sarshar S. Efficient synthesis of enantiomerically pure dihydropyrans Tetrahedron Letters. 46: 1281-1285. DOI: 10.1016/J.Tetlet.2004.12.128 |
0.431 |
|
| 2005 |
Hong B, Chen Z, Chen W, Sun H, Lee G. Traceless Solid-Phase Synthesis of Cyclopenta[c]quinolines and Cyclopenta[c]chromenes via Hetero [6+3] Cycloadditions of Fulvene. A Facile Approach to the 11-Heterosteroids Framework Journal of the Chinese Chemical Society. 52: 181-200. DOI: 10.1002/Jccs.200500028 |
0.411 |
|
| 2004 |
Hong BC, Wu JL, Gupta AK, Hallur MS, Liao JH. Azadiene Diels-Alder cycloaddition of fulvenes: a facile approach to the [1]pyrindine system. Organic Letters. 6: 3453-6. PMID 15387521 DOI: 10.1021/Ol048762C |
0.491 |
|
| 2004 |
Hong BC, Wu JL, Gupta AK, Hallur MS, Liao JH. Azadiene Diels-Alder cycloaddition of fulvenes: A facile approach to the [1]pyrindine system Organic Letters. 6: 3453-3456. DOI: 10.1021/ol048762c |
0.339 |
|
| 2004 |
Hong B, Gupta AK, Wu M, Liao J. Formal [6 + 3] Cycloaddition of Fulvenes with 2H-Azirine: A Facile Approach to the [2]Pyrindines System. Cheminform. 35. DOI: 10.1016/J.Tetlet.2003.12.105 |
0.357 |
|
| 2003 |
Hong BC, Gupta AK, Wu MF, Liao JH, Lee GH. Hetero [6+3] cycloaddition of fulvenes with N-alkylidene glycine esters: a facile synthesis of the delavayine and incarvillateine framework. Organic Letters. 5: 1689-92. PMID 12735753 DOI: 10.1021/ol034329b |
0.328 |
|
| 2003 |
Hong B, Chen S, Kumar ES, Lee G, Lin K. Intramolecular [2+2] Photocycloaddition-Fragmentation: Facile Entry to a Novel Tricyclic 5-6-7 Ring System Journal of the Chinese Chemical Society. 50: 917-926. DOI: 10.1002/Jccs.200300129 |
0.489 |
|
| 2002 |
Hong BC, Yeong-Jou S, Wu JL, Gupta AK, Lin KJ. Novel [6 + 2] cycloaddition of fulvenes with alkenes: A facile synthesis of the anislactone and hirsutane framework Organic Letters. 4: 2249-2252. PMID 12074679 DOI: 10.1021/ol026103z |
0.445 |
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| 2002 |
Hong BC, Shr YJ, Liao JH. Unprecedented microwave effects on the cycloaddition of fulvenes. A new approach to the construction of polycyclic ring systems Organic Letters. 4: 663-666. PMID 11843617 DOI: 10.1021/Ol017304Q |
0.462 |
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| 2001 |
Hong BC, Jiang YF, Kumar ES. Microwave-assisted [6+4]-cycloaddition of fulvenes and α-pyrones to azulene-indoles: Facile syntheses of novel antineoplastic agents Bioorganic and Medicinal Chemistry Letters. 11: 1981-1984. PMID 11454462 DOI: 10.1016/S0960-894X(01)00349-3 |
0.395 |
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| 2001 |
Hong BC, Shen IC, Liao JH. Unprecedented sequential oxidative dimerization and cycloaddition of 1,3-diketones to fulvenes. A facile synthesis of the cyclopenta[b]chromenes Tetrahedron Letters. 42: 935-938. DOI: 10.1016/S0040-4039(00)02139-0 |
0.391 |
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| 2000 |
Hong BC, Chen ZY, Chen WH. Traceless solid-phase synthesis of heterosteroid framework Organic Letters. 2: 2647-2649. PMID 10990418 DOI: 10.1021/Ol006180Z |
0.339 |
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| 2000 |
Hong BC, Sun HI, Shr YJ, Lin KJ. A novel oxidative alkylation-nitration of 1,3-dicarbonyl compounds to dicyclopentadiene and norbornene Journal of the Chemical Society, Perkin Transactions 1. 2939-2942. DOI: 10.1039/B004095I |
0.359 |
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| 1999 |
Hong B, Chin S. Bicyclo[3.2.1]octanes via McMurry Couplings Synthetic Communications. 29: 3097-3106. DOI: 10.1080/00397919908085933 |
0.366 |
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| 1999 |
Hong B, Sarshar S. RECENT ADVANCES IN THE SYNTHESIS OF INDAN SYSTEMS. A REVIEW Organic Preparations and Procedures International. 31: 1-86. DOI: 10.1080/00304949909355675 |
0.305 |
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| 1999 |
Hong B, Sun H, Chen Z. Unprecedented and novel hetero [6+3] cycloadditions of fulvene: a facile synthesis of the 11-oxasteroid framework Chemical Communications. 2125-2126. DOI: 10.1039/A906877E |
0.555 |
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| 1999 |
Hong B, Chen Z, Kumar ES. Unprecedented oxidative addition of α-halo acyl halides to 6,6-dialkoxyfulvene Journal of the Chemical Society-Perkin Transactions 1. 1135-1138. DOI: 10.1039/A902038A |
0.416 |
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| 1998 |
Hong BC, Hong JH, Tsai YC. Regio- and Enantioselective Prenyl Anion Transfer: Application to the Total Synthesis of (-)-Rosiridol. Angewandte Chemie (International Ed. in English). 37: 468-470. PMID 29711179 DOI: 10.1002/(Sici)1521-3773(19980302)37:4<468::Aid-Anie468>3.0.Co;2-Z |
0.464 |
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| 1997 |
Hong B, Hong J. A Simple and Cost Effective Synthesis of 2-Cyclopentadienyliden-1,3-Dioxolane Synthetic Communications. 27: 3385-3394. DOI: 10.1080/00397919708005639 |
0.462 |
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| 1997 |
Hong B, Chin S. Lanthanide(III) Promoted Aldol Condensation of Enones and Aldehydes1 Synthetic Communications. 27: 1191-1197. DOI: 10.1080/00397919708003356 |
0.421 |
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| 1997 |
Hong B, Sun aS, Tsai Y. Metal-Mediated [6 + 3] Cycloaddition Reactions of Fulvenes. A Novel Approach to Indan Systems Journal of Organic Chemistry. 62: 7717-7725. DOI: 10.1021/Jo970984J |
0.473 |
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| 1997 |
Hong BC, Hong JH. Sequential 'double-Michael' additions of dienolates to fulvene: Rapid access to the tricyclo[5.3.0.n2,5]alkane systems Tetrahedron Letters. 38: 255-258. DOI: 10.1016/S0040-4039(96)02275-7 |
0.4 |
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| 1996 |
Hong B, Sun S. Facile synthesis of azulenols: [6 + 4] cycloadditions of fulveneketene acetal Chemical Communications. 937-938. DOI: 10.1039/Cc9960000937 |
0.542 |
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| 1996 |
Hong BC, Sun SS. [6+3] cycloaddition of fulveneketene acetal Tetrahedron Letters. 37: 659-662. DOI: 10.1016/0040-4039(95)02226-0 |
0.442 |
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| 1995 |
Winkler JD, Hong B, Kim S, Lewin NE, Blumberg PM. On the Protein Kinase C Pharmacophore: Synthesis and Biological Activity of 4-Hydroxylated Analogs of Ingenol Synlett. 1995: 533-535. DOI: 10.1055/S-1995-5288 |
0.548 |
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| 1995 |
Winkler JD, Hong B, Bahador A, Kazanietz MG, Blumberg PM. Inside-outside stereoisomerism. VII. Methodology for the Synthesis of 3-Oxygenated Ingenanes. The First Ingenol Analogs with High Affinity for Protein Kinase C The Journal of Organic Chemistry. 60: 1381-1390. DOI: 10.1021/Jo00110A048 |
0.539 |
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| 1995 |
Winkler JD, Hong BC. Transannular radical reactions in bicycloalkanes with 'inside-outside' stereochemistry. An unusual bridgehead hydroxylation Tetrahedron Letters. 36: 683-686. DOI: 10.1016/0040-4039(94)02352-C |
0.568 |
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| 1994 |
Winkler JD, Henegar KE, Hong BC, Williard PG. Inside-outside stereoisomerism. 6. + synthesis of trans-bicyclo[4.4.1]undecan-11-one and the first stereoselective construction of the tricyclic nucleus of the ring system of the ingenane diterpenes Journal of the American Chemical Society. 116: 4183-4188. DOI: 10.1021/Ja00089A006 |
0.593 |
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| 1994 |
Corey EJ, Hong BC. Chemical emulation of the biosynthetic route to glycinoeclepin from a cycloartenol derivative Journal of the American Chemical Society. 116: 3149-3150. DOI: 10.1021/Ja00086A065 |
0.441 |
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| 1993 |
Winkler JD, Hong BC, Bahador A, Kazanietz MG, Blumberg PM. Synthesis of ingenol analogs wth affinity for protein kinase C Bioorganic and Medicinal Chemistry Letters. 3: 577-580. DOI: 10.1016/S0960-894X(01)81232-4 |
0.553 |
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| 1986 |
Fang J, Hong B. A Convergent Synthesis of (±)-Eldanolide Based on Reaction of Aldehyde with Dithio-Substituted Crotyllithium Compound Synthetic Communications. 16: 523-527. DOI: 10.1080/00397918608078766 |
0.456 |
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| Low-probability matches (unlikely to be authored by this person) |
| 2008 |
Hong BC, Wu MF, Tseng HC, Liao JH. Enantioselective organocatalytic formal [3 + 3]-cycloaddition of α,β-unsaturated aldehydes and application to the asymmetric synthesis of (-)-isopulegol hydrate and (-)-cubebaol Organic Letters. 10: 3651. DOI: 10.1021/ol060486+ |
0.295 |
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| 2020 |
Cheng LT, Luo SQ, Hong BC, Chen CL, Li WS, Lee GH. Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities. Organic & Biomolecular Chemistry. PMID 32735638 DOI: 10.1039/D0Ob01298J |
0.273 |
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| 2023 |
Huo SC, Indurmuddam RR, Hong BC, Lu CF, Chien SY. The hamburger-shape photocatalyst: thioxanthone-based chiral [2.2]paracyclophane for enantioselective visible-light photocatalysis of 3-methylquinoxalin-2(1)-one and styrenes. Organic & Biomolecular Chemistry. PMID 37987508 DOI: 10.1039/d3ob01580g |
0.268 |
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| 2003 |
Hong BC, Gupta AK, Wu MF, Liao JH, Lee GH. Hetero [6+3] cycloaddition of fulvenes with N-alkylidene glycine esters: A facile synthesis of the delavayine and incarvillateine framework Organic Letters. 5: 1689-1692. DOI: 10.1021/ol034329b |
0.252 |
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| 2010 |
Hong B, Sarshar S. ChemInform Abstract: Recent Advances in the Synthesis of Indan Systems Cheminform. 30: no-no. DOI: 10.1002/CHIN.199922254 |
0.236 |
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| 2018 |
Chao WC, Chiang TH, Chaudhari PD, Lin LJ, Lu JF, Hong BC, Wang JS, Lin TC, Shen JY, Chou PT. The azatryptophan-based fluorescent platform for in vitro rapid screening of inhibitors disrupting IKKβ-NEMO interaction. Bioorganic Chemistry. 81: 504-511. PMID 30245232 DOI: 10.1016/J.Bioorg.2018.09.006 |
0.217 |
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| 1998 |
Hong B, Hong J, Tsai Y. Ein regio- und enantioselektiver Prenylanion-Transfer und seine Anwendung bei der Totalsynthese von (−)-Rosiridol Angewandte Chemie. 110: 482-484. DOI: 10.1002/(Sici)1521-3757(19980216)110:4<482::Aid-Ange482>3.0.Co;2-B |
0.202 |
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| 2012 |
Hong B. Thank You, Yung-Son … Journal of the Chinese Chemical Society. 59: n/a-n/a. DOI: 10.1002/Jccs.201290009 |
0.194 |
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| Hide low-probability matches. |